Short communicationTransition metal-free and base-mediated transformation arylation of unactivated benzene with aryl halides in presence of N,N′-bis(salicylidene)ethylenediamine as organocatalyst-Science-Chemical Encyclopedia-lookchem

Short communicationTransition metal-free and base-mediated transformation arylation of unactivated benzene with aryl halides in presence of N,N′-bis(salicylidene)ethylenediamine as organocatalyst
Add time:08/28/2019 Source:sciencedirect.com

Direct transition metal-free arylation of benzene has been achieved using a combination of various aryl halides and N,N′-bis(salicylidene)ethylenediamine as a new ligand and catalyst. This facile one-pot reaction is reported as a new CH functionalization protocol for the synthesis of biaryls. In this research, 18-crown-6 and several Schiff-bases were tested and among them, N,N′-bis(salicylidene)ethylenediamine was found to be a great catalyst for this cross-coupling.

We also recommend Trading Suppliers and Manufacturers of N,N'-BIS(SALICYLIDENE)-1,3-PROPANEDIAMINE (cas 120-70-7). Pls Click Website Link as below: cas 120-70-7 suppliers

Prev:A proteome analysis of Corynebacterium glutamicum after exposure to the herbicide 2,4-dichlorophenoxy acetic acid (2,4-D)
Next: Aggregation-induced emission enhancement (AIEE) of N,N′-Bis(Salicylidene)-p-Phenylenediamine Schiff base: Synthesis, photophysical properties and its DFT studies)

Click to view details

Encyclopedia